Product image of Glucose B.Braun (Glucose Monohydrate) supplied by GNH India

Glucose B.Braun

Active Ingredient:
Glucose Monohydrate
Origin:
EU

Glucose B.Braun (Glucose Monohydrate)

Glucose B.Braun is a sterile aqueous solution containing glucose monohydrate, supplied for intravenous injection. It is a parenteral carbohydrate product marketed in the European Union and prescribed by health‑care professionals for rapid provision of glucose to support cellular energy and fluid balance. The formulation is isotonic and may include electrolytes to aid in maintaining plasma osmolarity during therapy. It is supplied in single‑use vials for safe handling.

Manufacturer / TM Owner

B.Braun Melsungen Ag

1
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Indications & Clinical Uses

Glucose B.Braun is used in clinical settings where rapid elevation of blood glucose or provision of an energy source is required.

  • Treatment of hypoglycemia when oral glucose is not feasible.
  • Component of parenteral nutrition regimens for patients unable to eat or absorb nutrients enterally.
  • Fluid replacement therapy to maintain intravascular volume and osmolar balance.
  • Support of electrolyte balance during surgery or critical care.
  • Adjunct in diagnostic procedures that require controlled glucose infusion.
  • Provision of glucose during prolonged fasting or pre‑operative preparation.

Side Effects

Intravenous administration of Glucose B.Braun can be associated with a range of adverse reactions, most of which are mild and transient, while rare events may be serious.

Common

  • Transient increase in blood glucose concentration that usually normalizes without intervention.
  • Mild irritation, redness, or discomfort at the intravenous infusion site.
  • Nausea, mild abdominal discomfort, or a feeling of fullness.
  • Fluid overload manifested as peripheral edema in patients with limited cardiac reserve.

Serious

  • Marked hyperglycemia that may precipitate osmotic diuresis and dehydration.
  • Allergic responses ranging from skin rash or urticaria to severe anaphylactic shock.
  • Significant electrolyte imbalances, such as hyponatremia, hyperkalemia, or shifts in calcium levels.

Precautions & Warnings

When prescribing Glucose B.Braun, clinicians should evaluate patient-specific factors and monitor for potential complications.

  • Assess baseline blood glucose and adjust infusion rate to avoid hyperglycemia.
  • Use caution in patients with diabetes mellitus, renal insufficiency, or congestive heart failure.
  • Monitor fluid balance and signs of overload, especially during prolonged infusions.
  • Verify compatibility with other intravenous solutions to prevent precipitation.
  • Observe for signs of allergic reaction during the first administration.
  • Adjust electrolyte supplementation as needed when large volumes are infused.

Avoid Interactions

Glucose B.Braun may interact with other intravenous medications or conditions that affect glucose metabolism.

Avoid

  • Concurrent administration with high‑dose insulin infusions without appropriate glucose monitoring.
  • Mixing with calcium‑containing solutions that can precipitate when combined with phosphate buffers.

Use with caution

  • Co‑administration with diuretics that may alter electrolyte status; monitor sodium and potassium levels.
  • Use alongside beta‑blockers, which can mask symptoms of hypoglycemia.
  • Infusion in patients receiving total parenteral nutrition containing other carbohydrate sources; adjust total glucose load.
  • Administration with glucocorticoids, which can raise blood glucose, requires closer monitoring.

Frequently Asked Questions

The active ingredient is glucose monohydrate, a simple carbohydrate used to provide energy when given intravenously.

Glucose B.Braun is supplied as a sterile solution for injection and is administered intravenously by a qualified health‑care professional.

It is indicated for treatment of hypoglycemia, as part of parenteral nutrition, for fluid replacement, and to help maintain electrolyte balance during surgery or critical care.

It can be used, but clinicians must closely monitor blood glucose levels and adjust the infusion rate to avoid excessive hyperglycemia.

Common side effects include transient hyperglycemia, mild infusion‑site irritation, nausea, and fluid overload in patients with limited cardiac reserve.

Serious reactions may include marked hyperglycemia with osmotic diuresis, allergic reactions such as rash or anaphylaxis, and significant electrolyte disturbances.

Compatibility should be confirmed; certain calcium‑containing solutions can precipitate when mixed with phosphate buffers, so they should be avoided.

Yes, especially in patients with heart failure or renal impairment; fluid balance should be monitored during infusion.

Large volumes can influence sodium, potassium, and calcium levels, so electrolyte monitoring is recommended during prolonged therapy.

Concurrent use is possible, but insulin dosing must be adjusted and glucose levels monitored to prevent severe hypoglycemia or hyperglycemia.

The product should be stored at controlled room temperature, protected from light, and used before the expiration date indicated on the vial.

Glucose B.Braun is a prescription‑only medication and must be prescribed by a qualified health‑care provider.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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